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黑色素瘤的前哨淋巴结活检:二十年经验后的最新进展。

Sentinel node biopsy for melanoma: an update after two decades of experience.

作者信息

Ross Merrick I

出版信息

Semin Cutan Med Surg. 2010 Dec;29(4):238-48. doi: 10.1016/j.sder.2010.11.002.

DOI:10.1016/j.sder.2010.11.002
PMID:21277537
Abstract

When detected and treated early, melanoma has an excellent prognosis. Unfortunately, as the tumor invades deeper into tissue the risk of metastatic spread to regional lymph nodes and beyond increases and the prognosis worsens significantly. Therefore, accurately detecting any regional lymphatic metastasis would significantly aid in determining a patient's prognosis and help guide his or her treatment plan. In 1991, Don Morton and colleagues presented new paradigm in diagnosing regional lymphatic involvement of tumors termed sentinel lymph node biopsy (SLNB). By mapping the regional lymph system around a tumor and tracing the lymphatic flow, a determination of the most likely lymph node or nodes the cancer will spread to first is made. Then, a limited biopsy of the most likely nodes is performed rather than a more-invasive removal of the entire local lymphatic chain. In 20 years that have followed, a great deal of information has been gained as to its accuracy, prognostic value, appropriate candidates, and its impact on regional disease control and survival. The SLNB has been shown to accurately stage regional lymph node basins in stage I and II melanoma patients with minimal morbidity. More sensitive histologic techniques are now being applied that may allow even greater accuracy in the staging of melanoma patients. Although specific percent risk thresholds are still in question, recommendation for SLNB when melanomas are 1 mm or thicker has gained wide acceptance. SLNB may also be appropriate for patients with melanomas that are between 0.76 and 1 mm thick and have ulceration, high mitotic rates, or reach a Clark level IV. Therefore, melanomas with IB or greater staging should be considered for SLNB.

摘要

若能早期发现并治疗,黑色素瘤的预后良好。不幸的是,随着肿瘤向组织深层浸润,发生区域淋巴结及远处转移的风险增加,预后也会显著恶化。因此,准确检测任何区域淋巴结转移对于判断患者预后及指导治疗方案具有重要意义。1991年,唐·莫顿及其同事提出了一种诊断肿瘤区域淋巴结受累的新方法,即前哨淋巴结活检(SLNB)。通过绘制肿瘤周围的区域淋巴系统并追踪淋巴引流,可确定癌症最有可能首先转移至的一个或多个淋巴结。然后,对最有可能的淋巴结进行有限活检,而非对整个局部淋巴链进行更具侵入性的切除。在随后的20年里,人们在其准确性、预后价值、合适的候选对象以及对区域疾病控制和生存的影响等方面获得了大量信息。前哨淋巴结活检已被证明能够以最小的发病率准确分期I期和II期黑色素瘤患者的区域淋巴结。现在正在应用更敏感的组织学技术,这可能会使黑色素瘤患者分期的准确性更高。尽管具体的风险百分比阈值仍存在争议,但对于厚度为1毫米或更厚的黑色素瘤患者进行前哨淋巴结活检的建议已被广泛接受。对于厚度在0.76至1毫米之间且有溃疡、高有丝分裂率或达到克拉克IV级的黑色素瘤患者,前哨淋巴结活检也可能适用。因此,分期为IB期或更高的黑色素瘤患者应考虑进行前哨淋巴结活检。

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